Allele Registry

Canonical Allele Identifier: PA2825060564

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV002115711

RCV003923632

ClinVar Variation:

1599190

HGVS (amino-acid)	Matching Registered Transcripts
NP_000131.2:p.Gly55Ser	CA8973304 NM_000140.5:c.163G>A